Tag | Content |
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EnhancerAtlas ID | HS073-14715 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:130307170-130308560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr9:130307978-130307995 | GAGAGGGCGGGGCTGAG | - | 6.34 |
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| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_00872 | chr9:130307100-130309530 | Adrenal_Gland | SE_01693 | chr9:130306961-130309439 | Aorta | SE_02373 | chr9:130307115-130309071 | Astrocytes | SE_02928 | chr9:130307014-130307921 | Bladder | SE_02928 | chr9:130307931-130309075 | Bladder | SE_06387 | chr9:130306787-130309382 | Brain_Hippocampus_Middle | SE_09759 | chr9:130307399-130308808 | CD14 | SE_23282 | chr9:130307005-130309400 | Colon_Crypt_1 | SE_23944 | chr9:130307025-130309323 | Colon_Crypt_2 | SE_25019 | chr9:130306996-130309121 | Colon_Crypt_3 | SE_26215 | chr9:130306862-130308979 | Duodenum_Smooth_Muscle | SE_26528 | chr9:130306979-130309763 | Esophagus | SE_30306 | chr9:130307079-130308183 | Fetal_Muscle | SE_30306 | chr9:130308225-130308976 | Fetal_Muscle | SE_31422 | chr9:130306988-130309744 | Gastric | SE_34381 | chr9:130307293-130309172 | HCT-116 | SE_34621 | chr9:130307025-130309715 | HeLa | SE_36116 | chr9:130306964-130309134 | HMEC | SE_37370 | chr9:130303549-130309613 | HSMMtube | SE_38118 | chr9:130307095-130309348 | HUVEC | SE_41594 | chr9:130306994-130309597 | LNCaP | SE_42140 | chr9:130306957-130309660 | Lung | SE_44201 | chr9:130306954-130309354 | NHDF-Ad | SE_44773 | chr9:130307002-130309462 | NHLF | SE_45705 | chr9:130295920-130309670 | Osteoblasts | SE_46654 | chr9:130307439-130308653 | Ovary | SE_47421 | chr9:130307032-130309038 | Panc1 | SE_47474 | chr9:130307029-130307910 | Pancreas | SE_47474 | chr9:130307913-130309626 | Pancreas | SE_50184 | chr9:130306967-130309642 | Sigmoid_Colon | SE_52096 | chr9:130306944-130309175 | Skeletal_Muscle_Myoblast | SE_52507 | chr9:130306965-130309353 | Small_Intestine | SE_53712 | chr9:130307483-130308862 | Spleen | SE_54748 | chr9:130301339-130309339 | Stomach_Smooth_Muscle | SE_55718 | chr9:130307336-130308761 | u87 | SE_63440 | chr9:130298563-130342452 | NCI-H69 | SE_63712 | chr9:130306930-130309344 | HSMM | SE_64980 | chr9:130307148-130308824 | NHEK | SE_65259 | chr9:130301019-130309850 | Pancreatic_islets | SE_67516 | chr9:130307336-130308761 | u87 | SE_68760 | chr9:130306962-130308837 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I127533 | chr9 | 130295863 | 130309594 |
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Enhancer Sequence | CCACTGGACC TGGGAAGGGA CCTCCAAGAT CAAGTCCAAA CTATCTTTTG GACAGATGGG 60 GAAACTGAGG CTGGGGAAAT GGGGAAAAGC TGCCCAGGGT CCCATTGCCC TGTTAGTGTC 120 CCAGCTCCTC TGAGACCATC TTGGGGAGAA ACAGGTGAAT GGGGCTTTCA CACCCAGCGA 180 ACCCAAGCGA ACCGCAACCT CAGCCCCTCA GCTTCCTCCT CAGCGGAGGA AATCTGGCCT 240 CTGGCCTTGG GGTCCCACGT CTACAGTGCC CTCCTAGCGT CCACCCCTTG TGCCTGGCCA 300 ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG CCACCTCCTC GGAACCCTCC CTCCAGACAA 360 GTCCCGGCCT CCCAGGTCTC CACAGCCTCC CTGGCCTCCA CTCCCACAGC CCCTGGCCTG 420 CTCCCCGGCA CTCCCCTCAA CCACAGTTAA TGCCTCATCT GAGACGCTCC CCGGACTGAG 480 ACTGCTCTCC GCTGTCTCCC CAGCACCCAG CTCCCGCCAG GCCCAGGGGG GTGCTTGATA 540 AACAAGTGCC GAACAAGTGT TAGGTCACCC AGCCTCAGGC GCCAAACAGG TCACCAGGGA 600 GGCCATGGTG GGCAGGGACT CAGTCTGAGG GCACAGGCCG TCTGGGTCTC ATCACAGAGG 660 CAGGTCAGGC CCAACAGAGC CAGGAGTCAG CTGGGGTTTT TCACAAGGCT GCCTTGAAAA 720 CTCTTCTCGG TTGGCAAATA TTTAACCAGG GCTGGGCCAC AACAGGTCTG GTGGGGAAGG 780 GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA 840 AATGCACCCA AAAAAACGGG TGACCCAAAA CCCGCCCACT GGGGCTGCCC TTTCCTTTAC 900 ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC ATTCCCATCT TGACACAAAC AGAAGGAAAC 960 AAAAGCCCTC TCATCCCCTC CTGCCCCCCA CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA 1020 CAGCCCACAG TGGCAGCTTG TTCTGGGAGC CCAGGATGAG GCATGCCTGC CGTCTGGGAA 1080 CACAGATCCT CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG GCCCCCAGCA GCGTCACCAC 1140 CCAGAGCAGG ACCCACACTC CAGGGGGTGG GCACCCAAGG CTGCCATCCT GCGGCCCCCT 1200 GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA TCTATGACAG TGATTGTGTA GACACGACCC 1260 TCCTTTCCTC TCACATGGAG TCACCCTTTC CTGTTGACTT TTTCTCCACA ATGTCTCTGG 1320 CCTTCATTCC TTTCTTGTCA TCCTCACCAC CCCCACAGGA GCCTGAGCCT TAGCCAGCCA 1380 CCTGTCAAAA 1390
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